TUCSON, Ariz. and DOWNINGTOWN, Penn., February 27, 2019 — Critical Path Institute’s (C-Path) Data Collaboration Center (DCC) and the Friedreich’s Ataxia Research Alliance (FARA) today announced the launch of the Friedreich’s Ataxia Integrated Clinical Database (FAICD). The new platform will enable collaborative research and data sharing to support the understanding of natural history, potential biomarkers and clinical endpoints, and promote research into novel clinical trial design in Friedreich’s ataxia (FA). By making this data available to researchers, the organizations hope to enable the development of tools that will help design and interpret efficient clinical trials — leading to effective treatments for FA as soon as possible.

“FA is a rare, progressive and fatal disease that affects multiple organ systems, and those living with the disease are in urgent need of effective treatments,” explained FARA’s Executive Director Jennifer Farmer. “FAICD addresses this need by providing a platform to share data and making it available to qualified researchers to expedite the drug development process. We believe this resource will inform and give future clinical trials of potential therapies the best chance of success.”

FAICD contains data contributed by collaborating companies that have carried out clinical trials in FA, as well as natural history and clinical outcome measure data from the Friedreich’s Ataxia Clinical Outcomes Measures Study (FACOMS) collected by the Collaborative Clinical Research Network in FA and funded by FARA.

All data contributed to this project is de-identified, mapped to standards defined by the Clinical Data Interchange Standards Consortium (CDISC) and curated by C-Path’s DCC before inclusion in FAICD.

“C-Path has a long history of expertise in data standards development, curation, and oversight of multiple data sharing initiatives,” said Richard Liwski, Director of the DCC and C-Path’s Chief Technology Officer. “We are proud to be part of the effort to coordinate collaborative contributions from data owners and integrate that data into a single database for this rare, degenerative and life-shortening neuromuscular disorder.”

Researchers interested in contributing data to FAICD and/or utilizing the database to advance FA-related research initiatives can learn more at https://cpathdev3.lotosnile.com/programs/dcc/projects/friedreichs-ataxia/.

About Friedreich’s Ataxia:
Friedreich’s ataxia (FA) is a debilitating, life-shortening, degenerative neuromuscular disorder. About one in 50,000 people in the United States has FA, with most having onset of symptoms between the ages of 5 and 18. Adult, or late-onset, FA is less common (less than 25 percent of diagnosed individuals), and can occur anytime during adulthood.

The signs and symptoms of Friedreich’s ataxia are:

• loss of coordination (ataxia) in the arms and legs
• fatigue, energy deprivation and muscle loss
• vision impairment, hearing loss, and slurred speech
• aggressive scoliosis (curvature of the spine)
• diabetes mellitus (insulin-dependent, in most cases)
• serious heart conditions, including hypertrophic cardiomyopathy and arrhythmias

The progressive loss of coordination and muscle strength leads to motor incapacitation and the full-time use of a wheelchair. Most young people diagnosed with FA require mobility aids such as a cane, walker or wheelchair by their teens or early 20s. There is presently no treatment for FA.